CVT-301
DrugLevodopa inhalation powder, will be supplied in capsules containing levodopa (l-dopa), designed to deliver to the lung using the CVT-301 inhaler.
NCT Number: NCT02633839
This is an open label, parallel group study to evaluate the pharmacokinetics (PK) and safety of a single dose of CVT-301 in smoking and non-smoking adults.
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Inclusion criteria
Exclusion criteria
Levodopa inhalation powder, will be supplied in capsules containing levodopa (l-dopa), designed to deliver to the lung using the CVT-301 inhaler.
Administered orally according to the carbidopa dosing schedule.
Other names: Lodosyn ®
Time frame: within 30 min prior to CVT-301 dose administration and specified time points up to 24 hours post-dose
Time frame: within 30 min prior to CVT-301 dose administration and specified time points up to 24 hours post-dose
Time frame: within 30 min prior to CVT-301 dose administration and specified time points up to 24 hours post-dose
Time frame: within 90 min prior to CVT-301 dose and at specified time points up to 24 hours post-dose
Pulmonary function will be measured by spirometry using the guideline specified by the Third National Health and Nutrition Examination Survey (NHANES III)
Time frame: up to 3 days
Acorda Therapeutics
Industry
A Phase 1 Study of the Safety and Levodopa Pharmacokinetics Following Single Dose Administration of CVT 301 (Levodopa Inhalation Powder) in Smoking and Non-Smoking Adults
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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